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BG10: Heterozygous frameshift mutation in glomulin causing autosomal dominant familial glomuvenous malformation with associated intracranial cavernoma
Publication year - 2021
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/bjd.20169
Subject(s) - frameshift mutation , medicine , mutation , genetics , biology , gene